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Job Description Are you ready to bring your expert clinical skills to a world-class facility recognized as top ten in the country for cardiology? Do you have a passion for the highest quality and patient happiness? Then please respond to this dynamic opportunity available with one of the best places to work in Southern California! We would be happy to hear from you. Cedars-Sinai Medical Center has been recognized as #1 in California and eight years in a row on the "Best Hospitals" Honor Roll by U.S. News & World Report, 2023- We are currently offering a $5,000 sign-on bonus to newly hired Techs! Summary of Essential Duties: * Assists with CVIC procedures applying approved protocols per standards of practice for safety, speed, organization, precision, and accuracy based upon the department's accrediting agency and/or department guidelines for exam protocols, adhering to department safety and productivity standards. * Scrubs, monitors, assists, and circulates safely and timely, supplying necessary equipment and performing vascular site management, while supporting FDA approved and clinical research procedures. * Performs all diagnostic tests, including coronary and structural heart intervention using electronic physiologic monitoring equipment and accurately records ECG, electrograms, hemodynamics, echocardiographic and other vital tracing obtained throughout the procedure. * Prepares and administers contrast and follows department procedures and guidelines in handling of contrast to maintain compliance with all safety requirements. Observes radiation and laser protection to regulatory safety requirements. * Performs sterile processing within guidelines for sterile field and equipment preparation, including inspection, counting, cleaning, patient and equipment transport, room stock, and documentation, with notification to supervisor and action needed for resolution. Sign-on bonus is available to newly hired Techs only. Current employees are not eligible. Qualifications Education: * High School Diploma or GED required * Successful completion of an Accredited CVT program with at least 800 hours of clinicals as part of that training program required License/Certifications: * Basic Life Support from the American Heart Association or American Red Cross required * ACLS preferred. ACLS is required if put into a Tech II position * RCIS preferred. RCIS is required if put into a Tech II position. Experience: * Previous Cath Lab experience preferred; graduates of a CV Tech program with no experience can be considered at the Tech I level * At least 3 years of Cath Lab experience required to qualify for Tech II position * Congenital Heart experience preferred #JOBS Keywords: Cardiac, Cardiovascular, Cath, Catheterization, Lab, Laboratory, Heart, Procedure, Tech, Technologist, Technician, Healthcare, Hospital, Medical Center, Los Angeles, CA, California Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

Job Description The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes. Join our team and use your skill with an organization known nationally for excellence in research! Are you ready to be a part of breakthrough research? Working independently but in close cooperation and in consultation with the Dr. Cingolani and other Research Scientists, the Postdoctoral Scientist will perform routine and complex laboratory procedures throughout training period. May develop, adapt, and implement new research techniques and protocols. Analyzes and interprets data. May assist in preparation of grant proposals. Participates in publications and presentations as author or co-author. Not responsible for generating grant funds. Primary Duties and Responsibilities: * May assist in the preparation of grant proposals, but is not responsible for generating grant funds. * May participate in publications and presentations as author or co-author. * Designs and performs experiments. Will keep appropriate experimental records and documentation and analyze the results with the PI. * Analyzes, interprets, summarizes, and compiles data. * Operates and maintains equipment and instruments. * May observe MD-patient or MD-human research subject interactions as it pertains directly to the research being performed. Qualifications Education: Acquires thorough technical and theoretical knowledge of research project and objectives during one to five (1-5) year post-doctoral appointment. * Works independently on research projects designed by a mentor (typically the PI) within the area of specialization. * Demonstrated aptitude to perform experimental protocols and procedures, including detailed data collection, and analysis, operation and maintenance of specialized equipment. * Excellent written and oral communication skills are essential. * Knowledge of safety standards. Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

Description The senior sleep technologist is to perform and evaluate routine and specialized overnight polysomnograms (PSGs), Multiple Sleep Latency Tests (MSLTs), and ensure patient safety. Major duties include calibrating equipment, attaching sensors to patients, performing bio-calibration, monitoring laboratory equipment, observing patients while they sleep, make decisions to initiate Bi/CPAP titration or other treatment should patients meet lab criteria, and score polysomnographic recordings on request. Occasionally work days to perform MSLTs, infant and pediatric recordings, scoring of records, daytime studies, and other functions as requested by the lab manager. Responsible to work at all UCLA Sleep Lab locations as needed for Laboratory operations. Level of effort (%) in specific activities related to scoring of records, performing daytime studies, and other functions. Level of effort (%) in specific activities noted in this job description may vary and may either increase or decrease depending on patient volume and Center needs. The sleep technologist reports to the Lab Manager and Supervisor, but may also receive instruction from Medical Director, staff physicians, or other designated personnel. The technologist should follow Laboratory protocols and policies for emergency situations as well as policies and procedures for reporting of non-emergency situations related to facilities, medical record, engineering, etc. The Technologist will work independently within their scope of practice and as a team member to ensure the smooth operation of the Sleep Disorders Center. Candidates will be placed according to their experience current career ladder level. Salary Range: $38.57 - 50.93/hr Senior Salary Range: $40.50 - 53.48/hr Qualifications * Polysomnography experience is required * Demonstrated ability to score 30 second epochs is required * Basic computer skills are required * CPR Certification is required * RPSGT certification is required * Other licensures/registrations as required by state departments or other licensing/accreditation agencies * Experience in sleep recording instrumentation and scoring techniques required. * Comfort working with clinical research populations required * Prior phlebotomy experience and certification preferred * Required to work flexible hours including nights and/or days as patient scheduling indicates UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person's unique achievements and experiences to further set us apart.

Job Description Principal Investigator, Dr. Warren G. Tourtellotte is looking for a Research Associate I to join the team! The Department of Pathology participates in the care of virtually every Cedars-Sinai Medical Center patient, using the most sophisticated methods for making accurate diagnoses in all areas of anatomic and clinical pathology. In addition, the department provides expert consultation services to the outside community. Our expert pathologists are committed to improving precision medicine approaches, advancing basic science and translational research, and providing excellent training and education. The Tourtellotte Lab studies gene regulation mediating sympathetic nervous system development, muscle stretch receptor morphogenesis and growth factor regulation, elp1 function in Familial Dysautonomia and neuron activity-induced gene regulation involved in learning and memory processing. Are you ready to be a part of breakthrough research? Working under direct supervision, the Research Associate I performs a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. Assists in general laboratory activities, including maintenance of reagents and stocking of supplies. Files and monitors documents. Keeps accurate and detailed records of experiments and results. Assists in the operation of specialized equipment and machinery. Observes safety standards and procedures. The Research Assistant I will be able to perform routine cellular, micro- and molecular biology procedures including, but not limited to Western, Northern blot, DNA/RNA, PCR, protein extraction, cell culture, Immunohistochemistry, and staining. This position does not have supervisory responsibilities. Primary Job Duties and Responsibilities: * Performs a variety of routine laboratory tasks and procedures. * Keeps accurate and detailed project records of experiments and results. * May assist with animal husbandry. * Maintains lab equipment and related records. * Transports, processes and logs samples. * Maintains computer database with relevant clinical information. * Performs lab maintenance duties, including glassware cleaning and sterilization. * Maintains stocks of general lab materials, and places orders for lab equipment and supplies. * Assists new students and fellows at the laboratory. * Assists in the operation of specialized equipment and machinery. * Observes and complies with safety standards and procedures. Qualifications Education: No experience is required. * Understanding of general research objectives. * Working knowledge of database management, personal computers, and presentation and imaging software. * Familiar with routine laboratory procedures and experimental protocols. * Must possess computer skills to include, but not limited to, Excel and Word. Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

Job Description The Department of Cardiology within the Smidt Heart Institute at Cedars-Sinai Medical Center is seeking a highly skilled and experienced leader in cardiovascular imaging to become the founding Director of the Division of Cardiovascular Imaging As the Director of the Division of Cardiovascular Imaging, you will provide visionary leadership for the establishment of one of the nation's most comprehensive cardiovascular imaging programs. In this role, you will oversee and continually advance the full spectrum of imaging services - including echocardiography, cardiac CT, cardiac MRI, and nuclear cardiology. You will lead a highly skilled multidisciplinary team of physicians, sonographers, technologists, nurses, and administrative staff, ensuring the seamless integration of cutting-edge imaging with world-class patient care. Your leadership will be central to driving innovation, maintaining the highest standards of diagnostic excellence, and optimizing operational performance across the entire imaging enterprise. Our current cardiovascular imaging sections and non-invasive echocardiography laboratory have a reputation for excellence in clinical care and research and have undergone enormous growth with our associated clinical cardiovascular programs. The visionary leader will have the opportunity to broaden and grow these sections and create new ones to encompass all disciplines of cardiovascular imaging. Cardiovascular imaging at Cedars-Sinai is a large and vibrant program that spans the main CSMC campus as well as affiliated sites. The Non-Invasive Echocardiography Laboratory alone performs more than 64,000 procedures each year - including transthoracic and transesophageal echocardiography, stress echocardiography, fetal imaging, and intracardiac studies - and is supported by 18 faculty echocardiographers, 43 sonographers, and a dedicated team of fellows, and other allied health professionals. In addition, the Cardiac Imaging Center performs over 20,000 studies annually and includes five faculty with expertise in cardiac imaging, two faculty with advanced training in congenital cardiac imaging, and a multitude of faculty engaged in research collaborations across multiple disciplines. This depth of clinical expertise and academic collaboration ensures comprehensive imaging capabilities for both adult and congenital populations. Furthermore, members of the imaging faculty have joint affiliations and leadership roles in the Cedars-Sinai Biomedical Imaging Research Institute (BIRI), which has established master and doctorate level training programs and whose faculty ranks include world-renowned scientists in advanced biomedical imaging. The Director will be responsible for guiding the growth of the entire Cardiovascular Imaging portfolio. The role includes fostering excellence in echocardiography, cardiac CT, MRI, and nuclear cardiology, and promoting collaboration across modalities to strengthen clinical integration. The Director will play an active role in selecting lab and section leaders and advancing research in cardiovascular imaging, mentoring fellows and junior faculty, and ensuring Cedars-Sinai continues to train and inspire the next generation of leaders in the field. Depending on interests and expertise, the position may also include direct participation in outpatient and/or inpatient clinical care. The Smidt Heart Institute is widely recognized as a leader in the delivery of cardiovascular care and a pioneer in the development of new treatments and diagnostic tools. Since 2018, Cedars-Sinai Cardiology/Cardiac Surgery was rated in the top three nationally in U.S. News and World Report Top Hospitals . The Department of Cardiology is one of the largest departments within the Cedars-Sinai Health System with over 170 faculty and has world renowned programs in cardiovascular imaging, advanced heart disease, interventional cardiology, cardiac electrophysiology, women's health, hypertension, and regenerative medicine. Ranked #1 in California* and on the "Best Hospitals" Honor Roll for eight years in a row , we are a national leader in providing high-quality, patient-centered healthcare that encompasses primary care as well as specialized medicine and conducting research that leads to lifesaving discoveries and innovations. Cedars-Sinai is one of the largest non-profit academic medical centers in the U.S., with 1,022 licensed beds, 2,993 physicians, 2,800 nurses and thousands of other healthcare professionals and staff. Cedars-Sinai Health System includes Cedars-Sinai Medical Center (our flagship hospital), the Academic Enterprise, Cedars-Sinai Marina del Rey Hospital, our ambulatory diagnostic and treatment centers, and our Medical Network. Recently, we have partnered with and added Torrance Memorial with its Medical Center and Medical Network as well as Huntington Hospital with its Medical Center and Medical Network to our system. The system comprises more than 2,300 beds and revenues exceeding $6 billion annually. It includes more than 50 outpatient venues spanning the entire region (e.g., Santa Monica and West Los Angeles, the South Bay, San Fernando Valley, and Pasadena). At Cedars-Sinai, we are caretakers and innovators committed to the pursuit of equitable healthcare. But health equity is not possible without representation. Our commitment to diversity goes beyond demographics or checking boxes. Our people must reflect the diverse identities, experiences and geographies of the communities and patients we serve - because that's what our patients, colleagues and communities deserve. Join us and take the next step of your career at Cedars-Sinai! Cedars-Sinai is in Southern California, surrounded by mountain ranges, valleys, forests, beautiful beaches along the Pacific Ocean, and nearby desert. L.A. is the entertainment capital of the world, a cultural mecca boasting more than 300 museums, and a paradise of beautiful weather. Diversity extends beyond geography to include one of the most ethnically and culturally diverse populations of any large city. In fact, Los Angeles is one of only two U.S. cities without a majority population. People from 140 countries speaking approximately 86 different languages call Los Angeles home. Our compensation philosophy: We offer competitive total compensation that includes pay, benefits, and other incentive programs for our employees. The total pay range shown takes into account the wide range of factors that are considered in making compensation decisions including knowledge/skills; relevant experience and training; education/certifications/licensure; and other business and organizational factors. This total pay range includes any incentive payments that may be applicable to this role. We also offer a comprehensive faculty benefits package. Pay Range: $538,639 - $822,138 Estimated Total Cash Compensation Qualifications Qualifications: * Medical Degree from an accredited medical school. * Board certification with the ABIM in Cardiovascular Disease. * Eligibility for an unrestricted California medical license. * Formal advanced training and demonstrated expertise in at least two cardiac imaging modalities (echocardiography, CT, MRI, or nuclear cardiology) is strongly preferred. * Eligible for appointment at the Professor level. * Established track record of excellence in clinical practice, research, and program leadership. Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

Description Under the supervision of an anesthesiologist, perform safe anesthesia care, consisting of the following: pre-operative assessment, writing of appropriate pre-op orders as specified by approved standard procedure, administration of all types of anesthetic and techniques, patient monitoring intra-operatively, provides for safe intra-op course and emergence and assists as necessary in post- operative care.You may be assigned to a 8, 10, or 12 hours shift, including evening, nights, weekends, and holidays. Work will be assigned to various OR's. This is a per diem role. Salary: $168.56/hourly Qualifications Required: Knowledge of current nursing, anesthesia and critical care techniques as evidenced by the following: Valid California RN and CRNA license- required Graduated from an accredited Master's orDNPprogram in Nurse Anesthesia -required Current certification/re-certification by the National Board of Certification & Recertification for NurseAnesthetists -required BLS and ACLS certifications from AHA or ARC -required Required: Ability to perform thorough pre, intra-operative, andpost-operative assessments and formulate safe anesthesia care plan. Required: Skill in performing pre-operative assessment of surgical and non-surgical patients, including: a. Identification of pre-existing disease entities and their potential impact upon anesthesia care and plan documentation of past medical history, physical examination, laboratory tests, ECG and chest X-ray b. Understanding interactions of pre-operative drug therapy with proposed anesthetic plan and agents for all age groups c. Identification of abnormalities on physical examination which pose potential problems in anesthesia management d. Understanding the medical indications for delay of elective surgery and for pre-operative specialty consultation Required: Ability to explain the proposed anesthetic technique, alternatives, risks and problems, thus obtaining proper documented legal informed consent prior to the administration of anesthesia. Required: Ability to properly and completely document significant information to form an anesthesia record of pre-operative, intra-operative and post-operative events. Required: Skill in determining safe airway management and interpretation of physiological monitoring. Abilityto interpret physiological data (ECG, BP, vital signs,PCWP, SVR) and adjustintervention to optimize patient safety in all age groups. Required: Ability to safely insert venous and arterial monitoring lines and devices under medical direction of anesthesiologist. Required: Knowledge of pharmacology, dosage, side effects and contraindications of all drugs currently employed in anesthesia practice atUCLA. Required: Skill in performing all techniques of MAC, regional and generalanesthesia commonly employed at UCLA for all age categories Required: Ability to recognize return of consciousness and reflexes signaling safe emergence from anesthesia, transport of patient to recovery room and informed report to qualified medical personnel who will assume care of the patient Required: Knowledge of current clinicaland theoretical education and research techniques as evidenced by experience,academic credential degree, and license.

Description Under the supervision of an anesthesiologist, perform safe anesthesia care, consisting of the following: pre-operative assessment, writing of appropriate pre-op orders as specified by approved standard procedure, administration of all types of anesthetic and techniques, patient monitoring intra-operatively, provides for safe intra-op course and emergence and assists as necessary in post- operative care. You may be assigned to a 8, 10, or 12 hours shift, including evening, nights, weekends, and holidays. Work will be assigned to various OR's. Salary range: $153.23/hourly Qualifications Required: Knowledge of current nursing, anesthesia and critical care techniques as evidenced by the following: Valid California RN and CRNA license- required Graduated from an accredited Master's orDNPprogram in Nurse Anesthesia -required Current certification/re-certification by the National Board of Certification & Recertification for NurseAnesthetists -required BLS and ACLS certifications from AHA or ARC -required Required: Ability to perform thorough pre, intra-operative, andpost-operative assessments and formulate safe anesthesia care plan. Required: Skill in performing pre-operative assessment of surgical and non-surgical patients, including: a. Identification of pre-existing disease entities and their potential impact upon anesthesia care and plan documentation of past medical history, physical examination, laboratory tests, ECG and chest X-ray b. Understanding interactions of pre-operative drug therapy with proposed anesthetic plan and agents for all age groups c. Identification of abnormalities on physical examination which pose potential problems in anesthesia management d. Understanding the medical indications for delay of elective surgery and for pre-operative specialty consultation Required: Ability to explain the proposed anesthetic technique, alternatives, risks and problems, thus obtaining proper documented legal informed consent prior to the administration of anesthesia. Required: Ability to properly and completely document significant information to form an anesthesia record of pre-operative, intra-operative and post-operative events. Required: Skill in determining safe airway management and interpretation of physiological monitoring. Abilityto interpret physiological data (ECG, BP, vital signs,PCWP, SVR) and adjustintervention to optimize patient safety in all age groups. Required: Ability to safely insert venous and arterial monitoring lines and devices under medical direction of anesthesiologist. Required: Knowledge of pharmacology, dosage, side effects and contraindications of all drugs currently employed in anesthesia practice atUCLA. Required: Skill in performing all techniques of MAC, regional and generalanesthesia commonly employed at UCLA for all age categories Required: Ability to recognize return of consciousness and reflexes signaling safe emergence from anesthesia, transport of patient to recovery room and informed report to qualified medical personnel who will assume care of the patient Required: Knowledge of current clinicaland theoretical education and research techniques as evidenced by experience,academic credential degree, and license.

Who We Are Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation's top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It's located in one of the world's safest and most economically vibrant communities and is Orange County's second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide. To learn more about UC Irvine, visit ___. UCI Health - Los Alamitos is a trusted full-service medical facility that has been part of the community for more than 50 years. We offer a wide range of services including 24-hour emergency care, cardiology, neurology, orthopaedics, women's health and senior health. As a DNV-GL designated Comprehensive Stroke Center, we provide advanced stroke care when it matters most. Our dedicated outpatient pavilion supports imaging, infusion and radiation oncology services. Whether you need specialized treatment or routine care, our expert team is committed to delivering high-quality compassionate care tailored to your needs. Your Role on the Team The position of Physician Assistant (PA) Day Shift n the Department of Medicine, Division of Hospital Medicine & Palliative Medicine, requires a highly competent, independent yet team-oriented individual who will be immersed in Hospital Medicine. Under the supervision of the Hospital Medicine & Palliative Medicine faculty and guided by the applicable policies and procedures, the Physician Assistant will participate in the comprehensive care of patients in the ambulatory or inpatient settings and provide multi- disciplinary care coordination, treatment, education, monitoring, and communication with patients and referring physicians. A PA is an Advanced Practice Provider (APP) who possesses the advanced education, knowledge, clinical skills and experience necessary to provide advanced nursing care in their area of specialization. This position may perform: • Functions as appropriate to their "scope of practice" (In general, the "scope of practice" includes the management of chronic stable medical conditions, routine care, acute or critical care, and medical and surgical procedures per their approved standardized procedure). Familiarity with state statute for their licenses is necessary., • Approved privileges are unique to each person and are unlikely to include ALL privileges, • The PA professional may provide patient care in age groups based on educational preparation and at all Health licensed settings and affiliates., • The PA has responsibility for the standards of care for their specified patient population and evidences self-direction and accountability both to quality of care and in the development of their role within the all Health locations and affiliates., • Advanced Practice Practitioners (APP) are required to be credentialed to practice and be privileged through Medical Staff to function in their clinical role. Credentialing and approval of privileges must be completed prior to the first working day., • The PA is accountable to, evaluated, and provided feedback by the supervising/collaborating physician, physician designee(s) in the same clinical specialty, or the Administrative Manager. POPULATION SERVED: Adult population What It Takes to be Successful Required: • Possess clear understanding of core internal medicine principles., • Knowledge of the elements of a medical history and skill in the history-taking process., • Expertise and appropriate physical exam skills., • Demonstrated experience in review and use of any standard protocols for Hospital Medicine patients., • Ability to establish and maintain effective working relationships across the program and UCI Health System., • Ability to exercise diplomacy and flexibility in interacting with physicians, nurses, other paramedical personnel, administrators, emergency and law enforcement officers., • Must demonstrate customer service skills appropriate to the job., • Skill to clearly communicate medical information to a broad variety of people, both in person and over the telephone., • Excellent written and verbal communication skills., • Writing skills to prepare clear medical reports, laboratory data and progress notes. Ability to maintain a work pace appropriate to the workload., • Must possess the skill, knowledge and ability essential to the successful performance of assigned duties., • Ability to be trained in the use of specialized medical equipment and procedures., • Demonstrates an understanding of and adheres to privacy, confidentiality, and security policies and procedures related to Protected Health Information (PHI) or other sensitive and personal information., • Licensure through the California Physician Assistant Board of the Medical Board of California as a physician assistant., • Must have a National Provider Identifier (NPI), or obtain an NPI, prior to employment start date and meet current Medicare requirements for billing., • Applicant must hold a current DEA Registration with schedules 2, 2N, 3, 3N, 4 and 5., • Current BLS certification and ACLS certification., • Experience in working with patients undergoing single and combined modality treatment plans. Preferred: • Multi-lingual Special Conditions: • Ability to obtain UCIMC Allied Health Professional Privileges prior to hire., • Applicant must provide documentation of provision of care (# and type of cases/procedures performed) during the past 24 months, representative of the scope and complexity of the privileges requested. Total Rewards In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our ___ and ___. Conditions of Employment: The University of California, Irvine (UCI) seeks to provide a safe and healthy environment for the entire UCI community. As part of this commitment, all applicants who accept an offer of employment must comply with the following conditions of employment: • Background Check and Live Scan, • Employment Misconduct*, • Legal Right to work in the United States, • Vaccination Policies, • Smoking and Tobacco Policy The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements. • California Child Abuse and Neglect Reporting Act, • E-Verify Closing Statement: The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the ___. We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming. UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824-0500 or . Consideration for Work Authorization Sponsorship Must be able to provide proof of work authorization

Description The incumbent will work as part of the TPCL team, which facilitates biomedical research by providing remnant human tissue samples and histology services. During surgeries, only a portion of the tissue removed from patients is used for diagnostic purposes; the remaining "remnant" tissue is typically discarded. The TPCL team collects, processes, stores, and distributes these remnant tissues to approved biomedical researchers at UCLA. Additionally, the team offers histology services, including embedding and sectioning of both frozen and formalin-fixed human and animal tissues, as well as digital imaging, image analysis, and immunohistochemistry. Key Responsibilities: • Receive tissue samples from clinical pathology staff for distribution as fresh tissues or for banking., • Freeze and/or process tissues in formalin, and document all samples banked or distributed., • Enter sample information into a secure database, ensuring accuracy and confidentiality., • Collaborate with pathology and frozen section room staff to expedite the delivery of surgical specimens., • Dissect surplus materials as trained. Histology Support: • Assist in processing formalin-fixed and fresh tissues for embedding (both in paraffin and OCT), sectioning (paraffin and frozen), and staining (H&E, special stains, immunohistochemistry, and immunofluorescence). • Prepare solutions, maintain laboratory equipment, and perform quality control procedures., • Evaluate the quality of tissue sections and stains, troubleshoot technical and equipment issues, and document all work performed. This role requires attention to detail, dedication to maintaining high-quality tissue samples, accurate data entry, and strict adherence to privacy and security protocols. Qualifications Maintains patient confidentiality at all times, following all appropriate federal, state and local regulations. Must have excellent English verbal, written and comprehensive skills Maintains a safe environment for others and self; adheres to all hospital safety regulations. Prior experience in a Pathology laboratory is preferred; on-site training will be available for the appropriate candidate, if necessary. Computer system knowledge (Microsoft Word and Excel) is required. BS/BA is preferred (Associates Degree in Science or equivalent with 3-5 years experience in Laboratory Science will be considered.) Must be able to pass the Medical Center physical exam upon hire.

Salary range: See Table 37B (). A reasonable estimate for this position is $76,700-$89,000. Open date: July 23, 2025 Most recent review date: Thursday, Apr 23, 2026 at 11:59pm (Pacific Time) Applications received after this date will be reviewed by the search committee if the position has not yet been filled. Final date: Tuesday, Jun 30, 2026 at 11:59pm (Pacific Time) Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled. The Division of Pulmonary, Critical Care, and Sleep Medicine, in the Department of Medicine at the David Geffen School of Medicine at UCLA, has openings for full-time Assistant Project Scientists. This position is intended for collaborative research working on lung injury, using a combination of in vitro systems, mouse models and human biospecimens. The study will initially concentrate on how complement proteins modulate the cellular response to injury. The candidate's work will focus on: 1) investigating immune responses at mucosal surfaces such as the lung and the gut using techniques such spectral flow cytometry, proteomic assays, confocal microscopy, and in vivo imaging in conditional knockout mouse models; 2) performing unbiased screens (such as CRISPR and high-throughput compound screens) to identify targets for modulating complement activity; 3) in vitro studies such as site-directed mutagenesis and immunoprecipitation-mass spectrometry to identify binding partners for proteins and how these affect cellular responses to stress; and, 4) developing new ex vivo models from human lung specimens for investigating the pathogenesis of lung injury and repair. with the goal of applying these techniques towards drug discovery. The candidate must also be able to analyze and interpret said data and use these to generate new ideas and hypotheses to move the project/field forward. Experience in analyzing unbiased datasets (for example, transcriptomic or proteomic data) and/or a background in structural biology is looked upon favorably. The Assistant Project Scientist will work in the Kulkarni Lab and serve as a lead for basic-translational lung injury project(s). The position involves in-person work in the Kulkarni Lab situated in the Clinical Health Sciences building at UCLA. The applicant will meet regularly with their PI, Dr. Kulkarni and other members of the lung injury working group. Responsibilities include: supporting the PI in the design and execution of funded projects by leading investigations in animal models of injury; developing new ex vivo models using mammalian lung tissue (including humans); incorporating new techniques into the workflow of the lab (e.g. multispectral flow cytometry, high throughput screening using cellular imaging, in vivo imaging in animals), tissue analysis by biochemical, proteomic, transcriptomic, metabolic and immunohistological approaches. The candidate will be responsible for identifying the best ways to execute the proposed questions being studied in the lab (along with the PI), identifying appropriate reagents to develop new techniques and assays and implementing and refining them to answer key questions, and perform logical series of experiments to develop understanding of the mechanism of action of intracellular and locally acting complement proteins, among other components of the host response. They will be responsible for co-mentoring other trainees in the lab, as well as assisting junior postdoctoral fellows, graduate students and undergraduate student researchers. Additional responsibilities include: Maintenance of laboratory logs and protocols to be compliant with UCLA protocols, preparing manuscripts for publication in scientific journals, and assisting the PI with the preparation of grant proposals. Required Qualifications: • Ph.D. in biomedical sciences or related field, • Minimum of 5 years of experience in biomedical research with a focus on a combination of immunology, plus: molecular biology, protein chemistry, structural biology, pharmacology, in vivo work in mouse models of injury, and/or working with primary cell culture systems (e.g., organoids, coculture systems). Required Skills: • Experience in immunology, and at least 2 years of specific experience working independently with experimental animals and primary cellular culture systems., • Experience in independently designing panels for multiparameter flow cytometry, acquiring and analyzing the data., • Experience in recombinant DNA technology, PCR, cell culture techniques, basic biochemistry, immunohistochemistry/immunofluorescence and animal models of disease., • Ability to handle several projects simultaneously., • Ability to train and advise laboratory personnel., • Ability to maintain and oversee the maintenance of high-quality scientific records. Specific Responsibilities: • Report directly to the Principal Investigator., • Carry out experiments and analyze the data generated with minimal supervision., • Oversee undergraduates, graduate students and new postdoctoral trainees in the lab., • Work on multiple projects efficiently and effectively., • Assist with preparation of grant proposals., • Deliver effective presentations and participate actively in weekly laboratory meetings., • Prepare manuscripts for publication in scientific journals., • Communicate effectively with other scientists worldwide., • Maintain or organize the maintenance of critical equipment, • Organize laboratory safety protocols and inventory systems The shared values of the DGSOM are expressed in the Cultural North Star, which was developed by members of our community and affirms our unswerving commitment to doing what's right, making things better, and being kind. These are the standards to which we hold ourselves, and one another. Please read more about this important DGSOM program at . Basic qualifications A Ph.D. in biomedical sciences or related field is required. Minimum of 5 years of experience in biomedical research with a focus on a combination of immunology, plus: molecular biology, protein chemistry, structural biology, pharmacology, in vivo work in mouse models of injury, and/or working with primary cell culture systems (e.g., organoids, coculture systems). Additional qualifications Experience in immunology, and at least 2 years of specific experience working independently with experimental animals and primary cellular culture systems. Experience in independently designing panels for multiparameter flow cytometry, acquiring and analyzing the data. Experience in recombinant DNA technology, PCR, cell culture techniques, basic biochemistry, immunohistochemistry/immunofluorescence and animal models of disease. Document requirements * Curriculum Vitae - Your most recently updated C.V. * UCLA Mission Statement - As the nation's premier public research university, UC's mission is the creation, dissemination, preservation and application of knowledge for the betterment of our global society. We have a particular responsibility to the people of the state of California which we express in the excellence of the education we provide, the impact of the research we do, the comprehensive, life-saving medical services we provide, and the public service mission we are devoted to. The University of California promotes the social mobility of its students, equips them with the tools and experience that furthers their ambitions, and regards their accomplishments across the life span as evidence of the profoundly positive impact of higher education. The UCLA campus has expressed these goals in its strategic plan as follows: -Deepen our engagement with Los Angeles -Expand our reach as a global university -Enhance our research and creative activities -Elevate how we teach -Become a more effective institution Prompt for candidates for recruitment: Reflecting on your personal and professional experiences, highlight your past contributions and future commitments to advancing UCLA's mission as embodied in the 2023-28 strategic plan. These accomplishments and ambitions may be discussed in the context of describing your teaching, scholarship, and service. Reference requirements none Apply link: Help contact: As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements. The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct. • "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer., • UC Sexual Violence and Sexual Harassment Policy, • UC Anti-Discrimination Policy for Employees, Students and Third Parties, • APM - 035: Affirmative Action and Nondiscrimination in Employment Los Angeles, CA

THE COMPANY Computrition, Inc. is the leading provider of fully integrated foodservice and nutrition management software systems. With over thirty years in the hospitality and healthcare industries, Computrition is an international company with offices throughout the United States and Canada. Computrition's all-encompassing software systems are designed to increase efficiency and productivity in the foodservice and/or nutrition services operation. We provide menu management, inventory control, nutrition office management, nutrient analysis, point of sale and more. Put your nutrition and food knowledge to use in a unique setting. Computrition allows you to creatively use computers in nutrition and food service. POSITION We are seeking a highly organized and proactive Technical Project Manager to lead and oversee research and development Cloud initiatives from concept through completion. This role is responsible for managing project scope, timeline, budget, and deliverables while ensuring alignment with strategic organizational objectives. The Project Manager will work cross-functionally with product development, engineering, operations, finance, and executive leadership teams to deliver innovative solutions on time and within budget. This is a full-time, remote position that reports directly to the business unit leader of the company. • Develop, implement, and maintain detailed project plans including timelines, milestones, resource allocations, and risk mitigation strategies., • Define project scope and objectives, ensuring alignment with business goals and stakeholder expectations., • Lead project kick-offs, regular status meetings, and post-project reviews., • Track project progress and deliverables through established project management tools and reporting systems., • Establish and manage project budgets, including forecasting, tracking, and reporting variances., • Ensure all project expenditures align with approved budgets and company financial policies., • Provide quarterly budget summaries and variance analyses to leadership teams., • Serve as the central point of contact for project-related communication across departments., • Prepare and present regular progress reports, dashboards, and executive summaries for leadership review., • Facilitate quarterly strategic reviews, providing updates on project status, key milestones, risks, and opportunities., • Proactively identify project risks, issues, and dependencies, developing mitigation and contingency plans., • Escalate critical issues promptly and facilitate resolution with appropriate stakeholders., • Contribute to the refinement of R&D project management processes, tools, and best practices., • Analyze project outcomes to identify lessons learned and opportunities for future improvement., • Bachelor's degree required. Prefer Bachelor's degree in Engineering, Business Administration, Project Management, or a related field ., • 5+ years of experience managing Cloud, product development, or technical projects preferred., • Experience working in a cross-functional team environment with both technical and non-technical stakeholders., • Strong understanding of Cloud and product development life cycles., • Proven ability to manage multiple complex projects simultaneously., • Excellent communication, organization, and presentation skills., • Proficiency in project management software (e.g., MS Project, Smartsheet, Asana, or similar)., • Fluency in technical software development terminology and tasks from a high level, • PMP or similar certification preferred., • Timely delivery of project milestones., • Budget adherence within approved tolerances., • Scope management and change control effectiveness., • Quality and innovation outcomes from R&D initiatives., • Stakeholder satisfaction and cross-functional collaboration. This is a full-time position. It is ideal for those who are self-motivated, dependable and stable. We offer a flexible schedule, excellent career growth opportunities and benefits package. If you feel that you are the A Team Player that we are looking for, please submit your resume and a one-page letter stating why you think you are the candidate that we are looking for. Salary is commensurate with experience. As part of Computrition's evaluation, candidates will be required to complete a background information check, prior to any offer being extended. #LI-RT1 Computrition401Regular Jonas Software is the leading provider of enterprise management software solutions to the Country and Golf Clubs, Foodservice, Construction, Fitness & Sports, Attractions, Salon & Spa, Education, Radiology/Laboratory Information Systems, and Product Licensing industries. Within these vertical markets, Jonas is made up of over 65 distinct brands, which are respected and leaders within their own domain. Jonas' vision is to be the branded global leader across the aforementioned vertical markets and to be recognized by customers and respective industry stakeholders as the trusted provider of 'Software for Life' and as an ambassador for technology, product innovation, quality, and customer service. Jonas Software is the valued technology partner of over 60,000 customers worldwide in more than 30 countries. Jonas employs over 2,000 skilled individuals consisting of a cross-section of industry experts and technology professionals. Jonas is headquartered in Canada and also operates offices throughout North America, the United Kingdom, Europe, Australia New Zealand and Africa. Jonas is a 100% owned subsidiary of Constellation Software Inc., headquartered in Toronto and traded on the S&P/TSX 60.

Salary range: $69,073 - $82,836 Open date: February 10, 2026 Most recent review date: Thursday, Apr 30, 2026 at 11:59pm (Pacific Time) Applications received after this date will be reviewed by the search committee if the position has not yet been filled. Final date: Sunday, May 31, 2026 at 11:59pm (Pacific Time) Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled. A postdoctoral position is available in the Lawrence Laboratory in the Department of Biological Chemistry at the University of California, Los Angeles (UCLA). The Lawrence Lab studies mechanisms of cellular stress response signaling at atomic, cellular and physiological scales. We are particularly interested in biochemical mechanisms defining how cellular stress response machinery senses and regulates cellular metabolic state, and how stress signaling drives cell-type-selective vulnerability in age-related neurodegenerative diseases. We welcome applications from motivated individuals interested biochemistry, structural biology, stem cell biology, or genomics/metabolomics-based projects. Currently, we are especially eager to hire a postdoc interested in defining mechanisms of integrated stress response regulation of mitochondrial biology in the context of Parkinson's Disease, for which we have dedicated funding beginning summer 2026. Responsibilities 1. In this role, the appointee will both lead their own project and be actively involved in teammates' projects, immerse themself at one of the world's leading institutions for biomedical research, and learn and teach skills in biochemistry, cell biology, structural biology, integrative physiology, and neuroscience., 2. The appointee will also have the opportunity to strengthen their leadership and collaboration skills by support in applying for fellowships and grants, interacting with graduate and undergraduate students, and taking leadership roles in manuscript preparation. More information can be found on the lab website: Lawrence-lab.org The successful candidate will benefit from a supportive lab environment and the highly collaborative UCLA community. Basic qualifications 1. Ph.D. degree in the field of cell biology, neuroscience, biochemistry, molecular biology, biophysics, genetics, or related disciplines * Curriculum Vitae - Your most recently updated C.V. * Statement of Research - Description of research interests and how they align with the Lawrence Lab mission * Reference check authorization release form - Complete and upload the reference check authorization release form * UCLA Mission Statement - As the nation's premier public research university, UC's mission is the creation, dissemination, preservation and application of knowledge for the betterment of our global society. We have a particular responsibility to the people of California which we express in the excellence of the education we provide, the impact of the research we do, the comprehensive, life-saving medical services we provide, and the public service mission we are devoted to. The University of California promotes the social mobility of its students, equips them with the tools and experience that furthers their ambitions, and regards their accomplishments across the life span as evidence of the profoundly positive impact of higher education. The UCLA campus has expressed these goals in its strategic plan as follows: Deepen our engagement with Los Angeles Expand our reach as a global university Enhance our research and creative activities Elevate how we teach Become a more effective institution Prompt for candidates for recruitment: Reflecting on your personal and professional experiences, highlight your past contributions and future commitments to advancing UCLA's mission as embodied in the 2023-28 strategic plan. These accomplishments and ambitions may be discussed in the context of describing your teaching, scholarship, and service Reference requirements As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements. The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct. • "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer., • UC Sexual Violence and Sexual Harassment Policy, • UC Anti-Discrimination Policy for Employees, Students and Third Parties, • APM - 035: Affirmative Action and Nondiscrimination in Employment Los Angeles, CA

Position title: Postdoctoral Scholar Salary range: The posted UC salary scales () set the minimum pay determined by rank and step at appointment. See Table 23: Postdoctoral Scholar-Employee, Postdoctoral Scholar-Fellow, Postdoctoral Scholar-Paid Direct, Fiscal Year Open date: July 8, 2025 Most recent review date: Thursday, Aug 7, 2025 at 11:59pm (Pacific Time) Applications received after this date will be reviewed by the search committee if the position has not yet been filled. Final date: Tuesday, Jun 30, 2026 at 11:59pm (Pacific Time) Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled. The G.O. Discovery Laboratory, invites applications for a Postdoctoral Scholar under the supervision of Professor Sanaz Memarzadeh, M.D., Ph.D. at the David Geffen School of Medicine at UCLA. The G.O. Discovery Lab is located within the UCLA Eli and Edythe Broad Cell Research Center, and is closely affiliated with the Jonsson Comprehensive Cancer Center and the Molecular Biology Institute. The G.O. Discovery Lab performs highly innovative and collaborative translational research with the potential to impact direct patient care by providing more effective therapies for women impacted by gynecologic cancers. This position is an excellent opportunity to join a highly energized research team and contribute to research projects funded by federal grants and other sources. For more information regarding the laboratory please visit . Applications are being sought from recent Ph.D. or M.D./Ph.D. graduates with a strong background in molecular biology, cancer immunology and translational research. Candidates are expected to have experience with conventional molecular biology techniques, microscopy, immunohistochemistry, FACS analysis, viral vectors, stem cells and genomics.. Experience with small animal surgical procedures are strongly preferred. The ideal candidate should be highly motivated and have publications in peer reviewed journals with at least two being the first author. The candidate will work closely with the PI and collaborators on research projects. The Postdoctoral Scholar will be expected to mentor trainees with the PI in the laboratory, gather and analyze data, prepare presentations, write manuscripts, and write and prepare grant applications. The posted UC salary scales () set the minimum pay determined by rank and step at appointment. See Table 23: Postdoctoral Scholar-Employee, Postdoctoral Scholar-Fellow, Postdoctoral Scholar-Paid Direct, Fiscal Year The shared values of the DGSOM are expressed in the Cultural North Star, which was developed by members of our community and affirms our unswerving commitment to doing what's right, making things better, and being kind. These are standards to which we hold ourselves, and one another. Please read more about this important DGSOM program at . The David Geffen School of Medicine Anti-racism roadmap is our co-created path to ensuring racial justice, equity, diversity and inclusion. We are committed to actively dismantling structural racism in our organization as described in more detail at: . Interested candidates can apply through the UC Recruit system located at: Basic qualifications Ph.D, MD., or M.D./Ph.D degree. Additional qualifications Candidates are expected to have experience with microscopy, immunohistochemistry, FACS analysis, virology, and immunology. Preferred qualifications Experience with small animal surgical procedures are strongly preferred. Document requirements * Curriculum Vitae - Your most recently updated C.V. * Letter of Interest * Reprint of 3 peer-reviewed publications in which the applicant is a co-author Reference requirements As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements. The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct. • "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, discrimination, dishonesty, or unethical conduct, as defined by the employer., • UC Sexual Violence and Sexual Harassment Policy, • UC Anti-Discrimination Policy for Employees, Students and Third Parties, • APM - 035: Affirmative Action and Nondiscrimination in Employment Los Angeles, CA

Description The Staff Research Associate (SRA) will work as part of a research team that will develop new expression systems for iPSC-derived neurons. Job duties include molecular cloning, mammalian cell culture, and basic molecular biology and biochemistry techniques (e.g. western blot and flow cytometry). The SRA will also be organizing and maintaining lab operations including stocking shelves, cleaning glassware, and other similar tasks. Please note, this is a full-time 4-5 month limited position and may convert to career. Salary range: $28.69 - $34.21/Hourly Qualifications Required: • Strong background in biology, • Experience with molecular cloning of constructs for transgene expression in iPSCs, • High level of scientific and professional integrity, • Ability to work alone and with a group, • Ability to establish and maintain excellent cooperative working relationship with supervisor and coworkers, • Ability to keep accurate and organized laboratory records, • Strong writing abilities, • Excellent attention to detail, • Working knowledge of iPSC transgene expression, • Strong quantitative backgroundPreferred:, • Minimum 1 year of experience/training.

Description Laboratory Assistant at Providence St. Joseph Medical Center in Burbank, CA. This position has multiple openings, per-diem and part-time and will work variable and day shifts. Providence St. Joseph Medical Center is proud to be Magnet recognized, the nation's highest recognition for nursing excellence. The American Nurses Credentialing Center's Magnet Recognition Program recognized the hospital's nursing team for exemplary patient care, nursing practice collaboration, patient outcomes and nursing research. In addition, Providence St. Joseph is recognized as one of the best regional hospitals in 11 types of care by U.S. News & World Report. Collects blood from patients, coordinates and processes specimen collection following established standards and practices. Providence caregivers are not simply valued - they're invaluable. Join our team at St Joseph Medical Center and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them. Required Qualifications: • Education to meet certification, license or registration requirement., • Phlebotomy experience. Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities. About Providence At Providence, our strength lies in Our Promise of "Know me, care for me, ease my way." Working at our family of organizations means that regardless of your role, we'll walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable. Posted are the minimum and the maximum wage rates on the wage range for this position. The successful candidate's placement on the wage range for this position will be determined based upon relevant job experience and other applicable factors. These amounts are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits. Applicants in the Unincorporated County of Los Angeles: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Unincorporated Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. About the Team The Sisters of Providence and Sisters of St. Joseph of Orange have deep roots in California, bringing health care and education to communities from the redwood forests to the beach shores of Orange county - and everywhere in between. In Southern California, Providence provides care throughout Los Angeles County, Orange County, High Desert and beyond. Our award-winning and comprehensive medical centers are known for outstanding programs in cancer, cardiology, neurosciences, orthopedics, women's services, emergency and trauma care, pediatrics and neonatal intensive care. Our not-for-profit network provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care, and even our own Providence High School. Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement. Requsition ID: 433435 Company: Providence Jobs Job Category: Clinical Laboratory Job Function: Clinical Care Job Schedule: Part time Job Shift: Multiple shifts available Career Track: Clinical Support Department: 7001 PSJMC CLINICAL LAB Address: CA Burbank 501 S Buena Vista St Work Location: Providence Saint Joseph Medical Ctr-Burbank Workplace Type: On-site Pay Range: $25.63 - $38.16 The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.

The candidate will conduct research in the laboratory of Dr.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description When you are part of the team at Thermo Fisher Scientific, you will do meaningful work, that makes a positive impact on a global scale. You will do challenging work and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best. You'll find the resources here to achieve your career goals and help take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. How will you make an impact? We are searching for an energetic Technical Sales Specialist ready to join our Thermo Fisher team! This role is responsible for the technical sales and related support activities for flow cytometry analyzers and cell sorters in specified academic, government and industrial accounts in the Western US. This role balances prospecting for new opportunities, demonstrating flow cytometry equipment, and participation in local scientific shows and events. We have TWO amazing openings (tied to this requisition) One managing the Southern California territory & One managing the Seattle territory. What will you do: The instrument portfolio contains innovative, high-quality flow cytometry instrumentation. Our business unit serves researchers worldwide, accelerating the process of scientific discovery with a strong focus on the areas of applied markets, cellular immunity and oncology. In this role you will be responsible for: * Demonstrating selling success in the area of flow cytometers with a primary focus on analyzers and cell sorters * Displaying an acute awareness of the life science marketplace, particularly within flow cytometry, its trends, and our competitors * Drive sales opportunities, including providing information on product capabilities and technical specifications, as well as instrument demonstrations * Attend and participate in sales meetings, seminars and trade shows Who are we looking for: * Bachelor's degree in Biology or related field required, preferred M.Sc. or PhD, * 5 years of technical experience in relevant scientific instrumentation, laboratory products, or life sciences field * Strong background in flow cytometry with a basic understanding of cell sorting * Hands-on experience in a research laboratory setting preferred, or previous sales experience selling instrumentation * Excellent presentation and communication skills, with ability to explain complex technical concepts * Strong understanding of laboratory workflows and customer requirements * Demonstrated success in meeting or exceeding sales targets preferred * Ability to work both independently and collaboratively in a matrix environment Knowledge, Skills, Abilities * Strong oral and written communication skills * Success in working and driving business growth across business functions * Ability to travel overnight up to 25% of the time * Valid driver's license and acceptable driving record * Able to lift 50 lbs. independently * Experience with Microsoft Office applications * Knowledge of CRM systems like Sales Force * Understanding of the sales funnel and how to move sales forward in a changing environment * Can-do demeanor and highly motivated to win sales and take share from competitors Benefits: * A choice of national medical and dental plans, and a national vision plan * Tax-advantaged savings and spending accounts and commuter benefits * Fleet vehicle * At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, short- and long-term disability, and volunteer time off in accordance with company policy * Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan About us: At Thermo Fisher Scientific, each one of our 120,000 outstanding minds has a unique story to tell. Join us and help fulfill our mission-enabling our customers to make the world healthier, cleaner and safer! Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Compensation and Benefits The salary range estimated for this position based in California is $83,300.00-$124,925.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: * A choice of national medical and dental plans, and a national vision plan, including health incentive programs * Employee assistance and family support programs, including commuter benefits and tuition reimbursement * At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy * Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan * Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Job Description The Applied Genomics, Computation & Translational Core is looking for a Biomedical Technician to join the team! Candidates with experience in single-cell and spatial assay technologies are highly desirable. This includes familiarity with techniques such as single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, multiplex imaging, and other high-dimensional molecular profiling platforms. A working knowledge of sample preparation workflows, library preparation, quality control metrics, and data generation associated with next-generation sequencing or imaging-based assays is strongly valued. Experience handling complex biological specimens and maintaining rigorous data integrity within high-throughput experimental environments is also preferred. The Cedars-Sinai Applied Genomics, Computation & Translational (AGCT) Core is an automated, high-throughput genomics facility equipped with the latest next-generation sequencing technologies. We specialize in single-cell and spatial omics, utilizing platforms including 10x Genomics (Chromium X, Xenium Analyzer, Visium CytAssist), Parse Biosciences, Scale Biosciences, Illumina, Singular Genomics G4X , and Bruker CosMX SMI. We also offer expertise in long-read sequencing via Oxford Nanopore Technologies (PromethION 24, MinION) and high-throughput short-read sequencing on the Illumina NovaSeq X Plus. We provide comprehensive support covering sample preparation, library construction, and diverse sequencing applications including bulk cell RNA-Seq, WGS/WES, ATAC-Seq, and metagenomics. The AGCT Core also delivers extensive bioinformatics analysis. Standard pipelines are established for primary data processing across all services, encompassing read alignment, quality control, expression quantification, variant calling, and peak calling. We also provide downstream analysis packages to help analyze these data in the context of the researcher's experimental design. We actively collaborate with investigators to develop sophisticated or custom computational solutions for specific research questions, including advanced analysis for spatial transcriptomics data. Our bioinformatics support extends to results interpretation, generation of publication-ready figures, and drafting manuscript methodology. To learn more please visit Applied Genomics, Computation & Translational Core | Cedars-Sinai. Are you ready to be a part of breakthrough research? The AGCT Core Biomedical Technician contributes to the laboratory sciences team of the lab. They work independently as part of a team under direct supervision of a team lead. The Biomedical Technician is responsible for performing laboratory benchwork strictly according to Standard Operating Procedures with accurate documentation and a theoretical understanding of assays utilized. They perform quality control on RNA and DNA samples, understanding the nuances of sample quality and qualifications. The Biomedical Technician contributes to the success of projects by providing good oral and written communication, documentation, and attentiveness to detail. They work with state-of-the-art technologies and instruments, performing next generation sequencing library preparation and sequencing. Primary Duties and Responsibilities * Performs a variety of project-specific process development tasks for multiple clients following standard operating procedures (SOPs). * Maintains good documentation in laboratory notebooks, data record/transfer, SOPs, and batch records. * Drafts standard operating procedures and maintains computer database. * Verifies samples received, logs samples into systems, and may transport to appropriate environment within the facility for storage following SOPs. * Performs lab maintenance duties, including glassware cleaning and sterilization. * Maintains lab equipment and related records. * Prepares cGMP production room, maintains material inventories, and places orders for equipment and supplies. * Assists in the operation of specialized equipment and machinery. * Ensures all activities comply with regulatory guidelines and safety standards, as appropriate. Department Specific Responsibilities * Construction of next generation sequencing libraries for bulk cell, single cell, and/or spatial omics using commercially available reagent kits. * Illumina short-read sequencing and/or Oxford Nanopore Technologies long-read sequencing of NGS libraries. * DNA/RNA QC via fluorescent quantification and automated electrophoresis. * Operation of state-of-the-art genomics equipment including NGS sequencers, automated liquid handlers, and tissue imagers, as well as standard laboratory equipment such as thermal cyclers, centrifuges, and qPCR machines. * Mathematical calculations, including fold dilution, normalization, and conversions. * Understand, analyze, and interpret DNA/RNA/NGS library/sequencing QC results. * Liaise with post-doctoral, doctoral, and staff researchers, clinical investigators, and principal investigators to provide quality customer service. * Handle multiple demands and/or manage complex and competing priorities, pivoting as needed based on current needs in a dynamic environment. * Apply advanced knowledge of science/learning/specialized intellectual instructions to analyze, interpret, or make deductions from varying facts or circumstances. * Provide and/or support a level of work excellence and accuracy; recognize and address flaws or errors that others may overlook. * Regular oral and written communication with team members and team lead. * Accurate and detailed electronic documentation of work performed and results obtained. * Work independently as part of a team under direct supervision of a team lead. * Observe and comply with all safety standards and procedures. Qualifications Required Qualifications * Associate Degree or College Diploma in Biology, Biochemistry, or a related scientific or engineering discipline. * Minimum of one (1) year of hands-on experience in a laboratory or biotechnology environment. * Demonstrated experience working with biomedical equipment, including routine maintenance, calibration, troubleshooting, and/or performance testing. Strongly Preferred * Experience with single-cell and spatial assay technologies. This includes familiarity with techniques such as single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, multiplex imaging, or other high-dimensional molecular profiling platforms. * Working knowledge of sample preparation workflows, library preparation, quality control metrics, and data generation associated with next-generation sequencing or imaging-based assays. * Experience handling complex biological specimens and maintaining data integrity in high-throughput experimental environments. * Bachelor's Degree in Biology, Biochemistry, or a related science or engineering field. Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

The position is located at the NASA Jet Propulsion Laboratory (NASA- JPL). Minimum of three (3) years of experience in operating and maintaining rotating equipment, preferably within a highly technical and research-oriented environment such as NASA JPL. Bizzell US has an immediate need for a Reliabi

Working under direct supervision, the Research Associate I will perform a variety of routine experimental protocols and procedures to support the objectives of one or more laboratory research projects in a specific area of research. Maintains stocks of general lab materials, and places orders for la

Orients research laboratory assistants or lower level research associates and undergraduate student researchers on day-to-day lab operations and routine procedures. We are seeking a Research Associate (Research Associate II) with experience in biochemistry, molecular biology, cell biology and/or pri

Plans and conducts research experiments in accordance with laboratory and safety protocols; independently performs non-routine and complex research laboratory procedures and techniques. USC Department of Medicine, Division of Oncology is seeking a Research Lab Tech III/Supervisor. Mohamed Abou-el-En

Conducts laboratory assignments, including assisting senior lab staff to carry out laboratory experiments. Orients research laboratory assistants or lower level research associates and undergraduate student researchers on day-to-day lab operations and routine procedures. The Associate will observe a

Job Description Grow your career at Cedars-Sinai! The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all our patients with cancer. Join our team and contribute to groundbreaking research. This position functions as a Clinical Research Coordinator providing support for clinical research protocols for the department. The Clinical Research Coordinator will assist the Research Department with all aspects of clinical research. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements. Primary Duties & Responsibilities * Perform accurate processing of research laboratory specimens while demonstrating a moderate degree of proficiency and understanding of research protocol and laboratory procedures, including centrifuging, aliquoting, storing, and shipping of specimens. * Monitor deliveries from sponsor, including inventory of kits, unpacking, and storing of supplies, and using kits and supplies appropriately for specimen collection, processing, storage, and shipping, as mandated by sponsor. Maintain electronic record of supplies. * Responsible for administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE's and source documents. * Facilitates screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process. * Coordinates logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. * Responsible for accurate and timely data collection, documentation, entry and reporting, including timely response to sponsor queries. * Schedules and participates in monitoring and auditing activities to ensure compliance, including implementing any corrective actions. * Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings. * Works closely with investigators and regulatory staff or directly with Institutional Review Board (IRB) to submit adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines. * Acts as a liaison with pharmaceutical company representatives or other project funding organizations to monitor and update project progress. * Provides assistance with research finance billing, including identifying and classifying routine care vs. research related care. * Attends meetings and conferences related to research activities, including research staff meetings. Participates in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested. Qualifications Educational Requirements: * High School Diploma or GED required. * Associate degree or college coursework in a related field (e.g., Life Sciences, Health Sciences, or similar) preferred. Licenses/Certification: * Current Certified Phlebotomy Technician I (CPT I) license issued by the State of California required. (Please note your license number in your resume and application) * Current Basic Life Support (BLS) certification from the American Heart Association or American Red Cross required. (Certification must be valid for at least 60 days beyond anticipated start date) Experience: * Minimum of six (6) months of healthcare-related or clinical research experience required. * Phlebotomy and/or laboratory assistant experience with demonstrated proficiency in applicable job responsibilities. * One (1) year of experience as a Clinical Research Coordinator, Clinical Research Associate, or Clinical Research Assistant preferred. **This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time. #Jobs-Indeed #LI-Onsite #LI-LA2 Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.

Job Description About the Role: The CLS Microbiologist plays a critical role in advancing microbiological research and analysis through the use of confocal laser scanning microscopy (CLSM). This per diem variable position focuses on the detailed examination and characterization of microbial communities, biofilms, and cellular structures to support scientific studies and product development. The successful candidate will be responsible for designing and executing experiments, analyzing complex data sets, and collaborating with cross-functional teams to interpret findings. Their work will directly contribute to improving understanding of microbial behavior and interactions in various environments, ultimately influencing innovation and quality control. This role demands a high level of technical expertise, precision, and the ability to communicate complex scientific information effectively to diverse stakeholders. Responsibilities • Operate and maintain confocal laser scanning microscopy equipment to capture high-resolution images of microbial samples., • Prepare and process biological specimens, including staining and labeling, to optimize visualization under CLSM., • Design and conduct experiments to investigate microbial structures, biofilm formation, and cellular interactions., • Analyze and interpret microscopy data using specialized software, generating detailed reports and presentations., • Collaborate with research scientists, quality assurance, and product development teams to integrate microbiological insights into projects., • Ensure compliance with laboratory safety protocols and maintain accurate documentation of experimental procedures and results., • Stay current with advancements in microscopy techniques and microbiological research to continuously improve methodologies.Requirements, • Bachelor’s degree in Microbiology, Biology, Biochemistry, or a related scientific discipline., • Hands-on experience with confocal laser scanning microscopy or similar advanced imaging technologies., • Strong understanding of microbiological techniques, including sample preparation and staining methods., • Proficiency in data analysis software relevant to microscopy imaging (e.g., ImageJ, Imaris)., • Excellent written and verbal communication skills to document and present scientific findings., • Preferred Qualifications:, • Master’s degree or higher in Microbiology, Cell Biology, or a related field., • Experience working with biofilms and microbial community analysis., • Familiarity with fluorescence labeling techniques and advanced microscopy modalities., • Knowledge of statistical analysis and experimental design in microbiological research., • Previous experience in a regulated laboratory environment such as pharmaceutical or environmental testing.Benefits, • Competitive hourly compensation: $55.00 - $62.00., • Flexible per diem variable work schedule offering work-life balance., • Exposure to cutting-edge microscopy technologies and collaborative scientific environment.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Key Responsibilities • Perform high‑complexity HLA testing, including:, • HLA typing (NGS, SSP, RT‑PCR platforms), • HLA antibody screening and identification (FlowPRA, Luminex, SAB), • Virtual and physical crossmatches, • Analyze, interpret, and document HLA test results in accordance with ASHI standards, • Prepare and process clinical and donor specimens (whole blood, serum, DNA, tissues), • Operate, maintain, and troubleshoot specialized HLA instruments such as:, • Luminex platforms, • NGS sequencers, • qPCR / amplification instruments, • Flow cytometers, • Perform quality control (QC), proficiency testing (PT), and maintain accurate documentation, • Assist with assay validations, method comparisons, and lot‑to‑lot verifications, • Participate in workflow improvement, troubleshooting, and CAPA activities, • Communicate effectively with team members, supervisors, and clinical partners, • Support training of new staff as needed, • Participate in rotational On-Call duties during weekends and holidaysQualifications Minimum Qualifications • One or more years of experience in an ASHI‑accredited HLA laboratory, • Familiarity with HLA testing workflows, including:, • HLA typing, • Flow cytometry crossmatches, • Luminex platforms (One Lambda), • Experience performing and interpreting SAB assays, • Understanding of virtual crossmatching and transplant matching algorithms, • Experience with LIMS/LIS systems commonly used in HLA labs, • Experience with method validations or data review Additional Information Compensation: • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job Description IVIRMA North America network of state-of-the-art fertility practices in the United States, is currently seeking an Andrology Lab Technician to join our growing Los Angeles, CA practice! This is a full-time position Monday-Friday 7am-3pm. The Andrology Laboratory Technician follows the laboratory’s procedures for specimen handling and processing, reporting and maintaining records of patient test results. Attention to detail is essential with these duties. The Andrology Lab Tech will be responsible for serving patients by providing precise and accurate laboratory results for the purpose of infertility assessment and management. This role is responsible for performing Andrology and Endocrine laboratory services in accordance with the Laboratory Procedure Manual. Essential Functions and Accountabilities: • Maintains accurate and current records of patient reports and inventory., • Adheres to the laboratory’s quality control policies; documents all quality control activities, as well as all instrument and procedural calibrations and maintenance performed., • Follows the laboratory’s policies and procedures whenever test systems are not within the laboratory’s established, acceptable levels of performance., • Studies and remains current and knowledgeable with the Laboratory Operating Manual regarding quality assurance, quality control, safety procedures and operating guidelines for performing all assigned laboratory services., • Holds a comprehensive understanding of and follow all OSHA requirements for safe laboratory operations to maintain a safe laboratory environment., • Assures quality care by adhering to therapeutic standards; follows practice, physician and laboratory division philosophies, as well as standards of care set by the state and other governing agency regulations., • Works cooperatively with the Company multidisciplinary teams to provide good patient care and achieves the objectives and goals of the practice., • Maintains patient confidence and protect operations by keeping all patient and proprietary information confidential. Adheres to signed HIPAA Confidentiality Agreement. Academic Training: • Bachelor’s Degree in a chemical, biological, clinical laboratory science or related – required, • Studies level: University Education (Bachelor's Degree), • Studies area: Chemical/Biological/Clinical Laboratory Science or other related field Position Requirements/Experience: • Minimum 6 months’ laboratory training towards degree or experience in a clinical or research lab – preferred Technical Skills: • Electronic Medical Records experience - preferred, • Excel at Microsoft Office Suites (Word, Excel, Power Point, Outlook), • Ability to operate laboratory equipment, hormone analyzers and microscopes IVI-RMA offers a comprehensive benefits package to all employees who work a minimum of 30 hours per week. • Medical, Dental, Vision Insurance Options, • Retirement 401K Plan, • Paid Time Off & Paid Holidays, • Company Paid: Life Insurance & Long-Term Disability & AD&D, • Flexible Spending Accounts, • Employee Assistance Program, • Tuition Reimbursement About IVIRMA Global: IVIRMA is the largest group in the world devoted exclusively to human Assisted Reproduction Technology. Along with the great privilege of providing fertility care to our patients, IVIRMA embraces the great responsibility of advancing the field of human reproduction. IVIRMA Innovation, as one of the pillars of IVIRMA Global, is a renowned leader in fertility research and science. Check out our websites at: & EEO “IVIRMA is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: IVIRMA is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at IVIRMA are based on business needs, job requirements and individual qualifications, without regard to race, color, religion and/or belief, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. IVIRMA will not tolerate discrimination or harassment based on any of these characteristics. IVIRMA encourages applicants of all ages.” Monday-Friday 7am-3pm

Job DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Research Associate, Discovery Biology and Pharmacology to work for a leading Greater Los Angeles area biologics company. Pay Rate: $25-35/hour depending on experience. Summary: The Research Associate, Discovery Biology and Pharmacology is a 6+ months temporary role with a possibility of conversion to full-time in our Research division. The position is in a dynamic and collaborative environment requiring a sense of urgency, excellent work ethic and the ability to work efficiently and accurately. Responsibilities: • Cell and tissue culture with sterile technique, • Culture, maintain, and perform experimental work with mammalian primary cells, tissues, and cell lines, • Work with peripheral blood mononuclear cells (PBMC), • Maintain experimental records and lab suppliesJob Requirements:, • Experience with the above responsibilities and the ability to work regular business hours in a temporary position in Monrovia, CA., • 6 months to 1 year laboratory experience in academia or industry., • A four-year degree is desired.

Job DescriptionJob Title: Research Associate - Biology - II Job Location: Santa Monica, CA Job Duration: 12 months (possible extension) Client name: Gilead Sciences Pay rate: $40.00-$49.00/Hour on W2 Shift time: Standard Shift Description: Key responsibilities: • Culture, quality control (QC), and cell banking of diverse solid tumor cell lines, • Engineer, culture and characterize CAR T cell function in vitro, • Perform routine laboratory procedures including ddPCR, qPCR, Flow, Luminex/MSD for ELISA and various cell-based immunoassays and biochemical assays, • Analyze, interpret, and translate results into actionable and tangible findings, • Maintain accurate and detailed records of laboratory procedures, experimental designs, and results in compliance with organizational standards; familiarity with Benchling a plus., • Design and execute fit-for-purpose or hypothesis-based experiments; analyze and, • interpret data to support development, • Communicate effectively research plans and results, in both oral and written form, • Coordinate tasks across multiple projects, work closely with cross-functional teams to support ongoing research projects, ensuring seamless integration of experimental findings, • Contribute to a dynamic, exciting culture that embraces teamwork and innovation OR Preferred Qualifications • BS 6+ years or MS 3+ years or equivalent degree of relevant experience in Cell Biology and/or Immunology., • Prior hands-on experience in the CAR-T field is preferred., • Proficiency in experiment design, data analysis, interpretation, and presentation. Required high degree of accuracy and attention to details., • Hands on experience with primary T cell isolation, culture and assays (e.g. cytotoxicity assays, cell proliferation assays, xCELLigence/eSight assays), multicolor flow cytometry,, • SCLC cell line culture and data analysis (FACSDiva, FlowJo, GraphPad, Prism, Excel)., • Experience with ex vivo CAR T manufacturing is preferred, • Strong communication skills, both written and verbal., • The ideal candidate should be flexible to meet team’s priorities and willing to support team members with their projects.#sczr2

Job DescriptionPhlebotomist & Laboratory Technician (Contract) Onyx Bio | Los Angeles, CA (Clinical Site-Based) About Onyx Bio Onyx is building a virtual immune system for faster and safer development of precision medicines. We generate rich, longitudinal multi-omics data in clinical context to deeply profile the progression of autoimmune diseases. As our biorepository grows, we apply advanced AI to immune data, using high-quality cell-based workflows to unlock new treatment and prevention strategies. Join us to help build the technical backbone that powers AI-driven insights into immune-related disease. Role Overview We’re looking for a contract Phlebotomist with experience as a Laboratory Technician to work on-site at a clinical study location in Los Angeles, approximately 3-5 mornings per week on an ongoing basis. You’ll perform venipuncture and process blood, tissue, and other biofluid samples according to SOPs. Full training will be provided on Onyx Bio’s specific sample processing protocols, including PBMC isolation, cryopreservation, and tissue processing. This is a hands-on, independent role—you’ll be the sole Onyx Bio presence at the site and need to execute reliably with minimal day-to-day supervision. Responsibilities * Perform venipuncture on study participants per protocol and collect blood into specified tube types. * Process blood and biofluid samples per SOP, including centrifugation, aliquoting, and pipetting. * Perform PBMC isolation, cryopreservation, and tissue processing procedures (training provided). * Perform cell counts and viability assessments using automated cell counter. * Label, log, and store all samples per study-specific chain-of-custody requirements. * Coordinate sample shipping: dry ice packaging, courier scheduling, temperature monitoring, and shipping documentation. * Maintain equipment (centrifuges, biosafety cabinet, cell counter) and flag maintenance needs. * Follow all SOPs, document deviations, and maintain accurate batch records. Requirements * California Certified Phlebotomy Technician (CPT-1 or CPT-2), active and in good standing. * 2+ years of phlebotomy experience in a clinical, research, or laboratory setting. * Basic laboratory bench skills: centrifugation, pipetting, aliquoting, and sample labeling. * Comfortable working independently at a clinical site without direct on-site supervision. * Strong attention to detail and ability to follow SOPs precisely. * Familiarity with universal precautions and safe handling of human biospecimens. * Must carry active professional liability insurance. * Must have an independently established business (LLC, sole proprietorship, or equivalent). Nice to Have * MLT (ASCP), MLS (ASCP), or California CLS credential. * Experience in a clinical research, biobank, or CRO setting. * Experience with PBMC isolation, cryopreservation, or cell counting. * Experience with cold-chain shipping logistics (dry ice, couriers). * IATA dangerous goods shipping certification. * Bilingual (English/Spanish). Training Provided Onyx Bio will provide hands-on training on all sample processing protocols, including PBMC isolation (Ficoll), cryopreservation with DMSO, tissue dissociation, and cell viability assessment. Candidates with careful laboratory technique and attention to detail will be fully trained to perform all required procedures. Compensation & Contract Terms $29–$39/hr depending on experience. LA-based, on-site at clinical location. Approximately 3-5 days per week, ongoing. This is a 1099 contract engagement. No benefits are provided. Team Values * Why not us? Why not now? Execute quickly and pragmatically to advance ongoing studies. * By any means necessary. Identify and implement practical solutions to keep trials moving. * Discomfort signals growth. Operate comfortably amid evolving protocols and processes. * Own outcomes. Take clear ownership of member experience and data quality, even as a contractor. * Faster together. Collaborate closely with the core Onyx team and fellow contingent staff. Equal Opportunity Onyx is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Job DescriptionDescription: Posterity Group LLC is a veteran owned, service-disabled small business, headquartered in Rockville, MD, that specializes in federal government contracting and staffing. We are tasked with staffing The VA Greater Los Angeles Healthcare System with Electroencephalography (EEG) Technicians. The EEG Technicians are expected to perform the following: This is a full-time position (40 hours per week) with standard hours of M-F 0700 to 1530 or 0730-1600 • Independently performs routine and non-standard procedures. (EEG and EP). These include Awake, Sleep, Portable, and ECS., • Independently perform routine and specialized procedures., • Independently perform routine long-term monitoring, LTM/CCTV – EEG monitoring. These include extended 10/20 electrode placement., • Performs as expert EEG technologist, maintaining state of the art quality in the principles, practices and procedures associated with Electroencephalography., • Consistently performs high quality studies for complex and non-routine procedures in difficult and demanding environments such as the operating room, research or intensive care environments., • All testing performed requires on-line analysis by the technologist to obtain the necessary data for correct diagnosis of the patient., • In all procedures, work closely with the physicians from Neurology Service and the Epilepsy Center of Excellence., • Follows established laboratory and/or hospital guidelines in completing “administrative duties” for each test performed., • Partly responsible for inventory of laboratory supplies. Requirements:, • At least 3 years of relevant experience, • Shall have a full, current and unrestricted license in any State, Territory, or Commonwealth of the United States or the District of Columbia) when services are performed onsite on VA property, • Certified by the American Board of Registration of EEG, CNIM and EP Technologists (ABRET) or the American Association of Electrodiagnostic Techs (AAET)., • Valid BLS

Job Description Job Title: Research Veterinarian Location: NHDP Vivarium, LSU School of Veterinary Medicine Annex, 5 Skip Bertman Dr., Baton Rouge, LA Position Summary: The NHDP is seeking a licensed veterinarian to provide professional veterinary care and oversight for a specialized research animal colony composed of armadillos and mice. This position supports leprosy (Hansen’s disease) research through collaboration with NIAID and requires expertise in exotic animal medicine, research compliance, and laboratory animal welfare. Key Responsibilities: * Conduct monthly on-site visits to inspect facilities, provide preventative care, and consult with staff * Provide 24-hour availability for emergency consultation and treatment * Perform scheduled and unscheduled advanced treatments, including survival surgeries * Dispense and manage DEA-controlled substances as needed * Conduct semiannual program reviews and facility inspections per NIH Office of Laboratory Animal Welfare standards * Diagnose, treat, and control diseases in research animal colonies Required Qualifications: * DVM or equivalent from an AVMA-accredited institution * Valid veterinary license in the United States * Experience with exotic species and research animals (e.g., armadillos, immunocompromised mice) * Familiarity with federal animal welfare regulations, including IACUC responsibilities * Ability to dispense and manage DEA-controlled substances Powered by JazzHR 3cvrwtfsE2

Job Description Position Responsibilities: * Work from preliminary design drawings, sketches, blueprints, schematics, and both verbal and written instructions to determine the most appropriate methods for integrating designs and meeting production and laboratory requirements. * Perform assembly and integration tasks to precise tolerances, using expertise to select the most effective methods for meeting engineering specifications. * Operate specialized equipment during spacecraft assembly, such as hydraulic test consoles, cooling system test consoles, alignment fixtures, and installation fixtures. * Determine the sequence of operations and install components in space vehicles before testing, including performing complete system leak and pressure checks, as well as alignment checks of control surfaces. * Handle fragile multi-layer insulation (MLI) films and materials with care during installation onto test and flight articles. * Support the installation of MLI and SLI (Solid-Layer Insulation) on spacecraft, ensuring all procedures meet required specifications. * Assist engineers and research staff in identifying improved procedures and perform assigned duties at specific test stations. Record and analyze test data, generating reports, charts, and graphs. * Acquire necessary certifications and perform incidental related duties and rework as needed, all with minimal supervision. * Demonstrate thorough knowledge of applicable materials and process specifications. * Provide instruction, guidance, and support to colleagues in the same or other related classifications. * Apply comprehensive knowledge of mechanical principles to perform all tasks. * Support range operations, including tests, integration, and hardware moves. * Operate computer-controlled equipment, including heated tools, ovens, positioners, alignment systems, lift equipment, cranes, and hand and power tools. * Other duties as assigned. This position is expected to be 100% onsite. The selected candidate will be required to work onsite at one of the listed location options. Security Clearance and Export Control Requirements This position must meet Export Control compliance requirements, therefore a “US Person” as defined by 22 C.F.R. § 120.15 is required. “US Person” includes US Citizen, lawful permanent resident, refugee, or asylee. Basic Qualifications (Required Skills/Experience): * High School Diploma or GED * Minimum of 4 years of relevant experience in mechanical assembly for high-reliability products * Proven experience in building and terminating wiring harnesses to a high standard for racks and boxes * Experience using a variety of hand tools, including scalpels, scissors, hollow punches, etc. * Skilled in interpreting mechanical drawings, schematics, and harness wiring diagrams, as well as internal and external specifications * Proficient in using inspection tools such as calipers, micrometers, and digital multimeters (DMM) * Experience with assembly tooling and/or composites fabrication and assembly * Proficient in using various hand and power tools * Experience with mixing epoxy materials Preferred Qualifications (Desired Skills/Experience): * Minimum 5+ years of Integration experience * At least 1 year of experience working with MLI/thermal blankets. * Certification to J-STD-001 space, NASA.STD.8739.4 * Demonstrated exceptional attention to detail * Excellent communication and teamwork skills * Experience working in a clean room environment * Ability to generate discrepancy reports as they occur in areas of influence * Proficient with Microsoft Word, Excel, and PowerPoint * Open to travel * Active Security Clearance Conflict of Interest: Successful candidates for this job must satisfy the Company’s Conflict of Interest (COI) assessment process Drug Free Workplace: Millennium Space Systems, a Boeing Company, is a Drug Free Workplace (DFW) where post offer applicants and employees are subject to testing for marijuana, cocaine, opioids, amphetamines, PCP, and alcohol when criteria is met as outlined in our policies. **Additional Information: ** * This is a union-represented position * This is an hourly position governed by the Cabinet Makers, Millmen and Industrial Carpenters Union (CMM&IC Local 721) * The selected candidate must be able to work any shift, as assigned. * New hires and employees transferring from non-union roles may be required to attend or complete training within their 90-day probationary period. Continued employment is contingent on successfully completing the probationary period. Shift: At Millennium Space Systems, a Boeing Company, we strive to deliver a Total Rewards package that will attract, engage and retain the top talent. Elements of the Total Rewards package include competitive base pay and variable compensation opportunities. Millennium Space Systems also provides eligible employees with an opportunity to enroll in a variety of benefit programs, generally including health insurance, flexible spending accounts, health savings accounts, retirement savings plans, life and disability insurance programs, and a number of programs that provide for both paid and unpaid time away from work. The specific programs and options available to any given employee may vary depending on eligibility factors such as geographic location, date of hire, and the applicability of collective bargaining agreements. Pay is based upon candidate experience and qualifications, as well as market and business considerations. Summary Pay Range: Grade 24: $29.42/hr - $47.09/hr Millennium is DDTC-registered, ITAR-compliant Company. This position is located at a facility that requires special access. Applicants MUST be U.S. citizens and eligible for a security clearance. Additionally, applicants must be willing to apply for and maintain a security clearance. We encourage all interested candidates to apply for any open position for which they feel they are qualified. Language Requirements: Not Applicable Education: High School Diploma or Equivalent Relocation: Relocation assistance is not a negotiable benefit for this position. Security Clearance: This position requires the ability to obtain a U.S. Security Clearance for which the U.S. Government requires U.S. Citizenship. An interim and/or final U.S. Secret Clearance Post-Start is required. Visa Sponsorship: Employer will not sponsor applicants for employment visa status. Contingent Upon Award Program This position is not contingent upon program award Shift: Shift 2 (United States of America) Stay safe from recruitment fraud! The only way to apply for a position at Boeing is via our Careers website. Learn how to protect yourself from recruitment fraud - Recruitment Fraud Warning Boeing is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national origin, gender, sexual orientation, gender identity, age, physical or mental disability, genetic factors, military/veteran status or other characteristics protected by law. EEO is the law Boeing EEO Policy Request an Accommodation Applicant Privacy Boeing Participates in E – Verify • E-Verify (English), • Right to Work (English), • Right to Work (Spanish)

Job Description ABOUT THE COMPANY Camden Center is a partial hospitalization and intensive outpatient treatment center that offers comprehensive, multi-disciplinary treatment for psychiatric and addictive disorders. Our staff is comprised of nationally recognized medical doctors, psychotherapists, and integrative medicine specialists who have been recruited as experts in their field to work with our patients. Camden Center is a medical organization established and operated by physicians, and is founded on the principles of clinical excellence, compassionate care, and respect for our patients. ABOUT THE POSITION The administrative assistant position is an entry-level position, ideal for motivated new talent who have a strong interest in the mental health field and/or want to grow into a senior administrative role. If you are interested in a mental health career, this role will provide you with unparalleled access to clinical meetings, where you will learn how experts in psychiatry, psychology, and social work approach and implement best-in-class treatment for our patients. If you are interested in an administrative career, you will appreciate that one of our company values is nurturing and developing our employee’s careers, which is why we have a proven track record of identifying internal talent and promoting within. RESPONSIBILITIES: The administrative assistant will be expected to provide clerical support to all Camden Center staff. The administrative assistant will also be responsible for greeting visitors as they arrive, directing them to various offices when appropriate, and maintaining a welcoming environment. Core duties and responsibilities include: • Answer phones, transfer calls to the appropriate station, and take detailed messages as needed; differentiate urgent messages and regular calls that can be returned at the end of the day, • Manage calendars for patients and staff, • Compose emails to patients, staff, and associates with professionalism, • Use discretion and good judgment in handling sensitive and confidential information, • Follow all HIPAA regulations, requirements, and guidelines, • Organize patient files and information into Medical Records Database and Google Drive, • Take inventory of office and clinical supplies and place orders/restock as needed, • Maintain cleanliness and upkeep of common areas and therapy offices, • Prioritize multiple tasks, meet deadlines, and maintain excellent attention to detail, • Collect samples and prepare urinary analysis screenings for laboratory testing, • Distribute medication and take vitals as directed by the medical team, • 1-3 years of administrative experience, • Strong computer and internet research skills; proficiency in the use of Google Workspace, • Professionalism of the highest caliber in all interactions with patients and staff, • Excellent interpersonal skills, • Ability to work well with all levels of management, staff, patients, and vendors, • Must be able to legally work in the United States and provide documentation (2 forms of ID and/or Green Card), • Must be able to sit and stand at length (up to 4-hours), • Must be able to lift, push, and pull up to 25-pounds, • Must be able to kneel, bend, and squat 40 hours/week. Pay range is $22.00/hour - $25.00/hour. Benefits for full-time employees include medical, paid and sick time off, matching 401(k), holiday pay, and a flexible spending account. Job Type: Full-time Keywords: administrative, healthcare, mental health, therapy, treatment center Powered by JazzHR pNGl2FSKpQ

Job Description Imaging Scheduler (Radiology Scheduler) Job Description Beverly Hills Cancer Center vigorously strives to be among the world's best health centers in our pursuit of total health and wellness by delivering leading-edge medicine in a truly compassionate manner. By combining breakthrough research with advanced diagnostic technologies and a variety of treatment modalities, our dedicated medical professionals provide uniquely comprehensive care to those with cancer and other life-threatening diseases. Our spacious, modern facility offers state-of-the-art medicine in an aesthetic, comfortable environment. If you are looking for an amazing opportunity at the top health center to help patient care, please apply today. ESSENTIAL DUTIES • Plan, organize, direct and schedule patient's internal appointments based upon orders, for different imaging/radiology modalities., • Coordinate and track external referrals., • Verification of Insurance and entering information into EMR., • Requesting Authorizations., • Coordinate obtaining and sending medical records requested., • Monitor daily clinic schedules in accordance with scheduling protocols., • Provide strong alliance and acts as a liaison with all medical staff (including physicians) and all ancillary departments of BHCC., • Excellent customer service skills and communication skills., • Bachelor's degree required., • Minimum of two years of patient scheduling experience and knowledge of insurance verification/authorization process required., • Imaging/radiology experience required., • Excellent computer skills and EMR knowledge. We offer competitive salaries and a diverse blend of benefits and incentives. Benefits include: • Health, dental, and vision insurance, • 401k matching, • FSA, • Company-sponsored life insurance, • Voluntary supplemental life insurance, • Voluntary short-term / long-term disability options, • Flex PTO & paid holidays, • Employee recognition programs, • Team building events & employee appreciation lunches, • Referral bonus programs At the Beverly Hills Cancer Center, our primary goal is to cure every patient's cancer. Since we know that in many cases advanced-stage cancers cannot be cured, our next goal is to make cancer a chronic disease, with which our patients can live and lead relatively normal lives. We accomplish our goals daily in our Los Angeles facility, which provides state-of-the-art, cutting-edge medical treatment, and caring attention to the mind, body and soul of each and every patient. With this fusion of science and caring, we aim to provide our patients with the best possible healing, and pride ourselves for being one of the best cancer treatment centers internationally. As a private, comprehensive facility, Beverly Hills Cancer Center provides state-of-the-art cancer treatment under one roof. Our facilities include an innovative radiation oncology center, a soothing and spacious infusion center, a full-service diagnostic imaging center (with MRI, CT, PET/CT, and Bone Scan technology), and a complete, award-winning diagnostic laboratory. We also conduct some of the world’s leading clinical trials for cancer treatment right here in our facility — making ours one of the top cancer centers in Los Angeles and worldwide. Driven by our unique model and goal to provide exceptional and personalized care, we have become the only private comprehensive cancer treatment facility in Southern California. By combining advanced treatment modalities and technologies, in a soothing environment with caring physicians and staff, we are able to provide maximum peace of mind for patients. While such things may seem like a luxury to some, here at the Beverly Hills Cancer Center we understand that a tranquil, stress-free environment is integral to the healing process. Beverly Hills Cancer Center provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to, internal equity, experience (including specific industry), education, specialty and training. This pay scale is not a promise of a particular wage.

Job Description Are you in search of a fulfilling and meaningful position? Do you want to work for an organization that promotes growth and development? Here at Men's Health Foundation we envision a world where inequity and stigma do not separate people from healthcare. "Reimagining Healthcare" is our commitment to affirming the unique experience of every patient. We prioritize our patients’ evolving needs and strive to help each patient feel comfortable, understood, and respected. Why Men's Health Foundation? Men's Health Foundation is seeking compassionate, mission-driven individuals. We believe that by reimagining how healthcare is delivered, we can help create greater health equity for those most at risk, breaking down barriers to care. We welcome all backgrounds, gender identities, and expressions. We recognize our staff as the heart of our organization and seek to provide a generous and competitive benefits package to support our employee's well-being. We offer the following: • Medical, Dental, Vision, Life and LTD insurance (may be eligible on the 1st of the month following date of hire), • 12 Paid Holidays (including 1 mental health day), • 401(k) Retirement plan (may be eligible for employer matching up to 4% following completion of 90th day of employment), • Flexible Spending Account (FSA), • 40 hours of sick pay (following completion of 90th day of employment) Organization Background Men’s Health Foundation connects men at risk to comprehensive healthcare and wellness through education, collaboration, and advocacy. Inspiring and empowering all men to live longer, healthier, and happier lives. We see a world where inequity and stigma do not separate men from healthcare. At Men’s Health Foundation, we are reimagining men’s healthcare. Founded in 1999, Mills Clinical Research (MCR) conducts cutting-edge research with a special focus on infectious diseases including HIV prevention and treatment, vaccine trials, medical device trials, and trials focused on men’s health. Mills Clinical Research is led by Dr. Anthony Mills as the CEO and Primary Investigator (PI) with office locations in West Hollywood and South LA. MCR is affiliated with Men’s Health Foundation and has expansive community networks within Southern California. They share the mission to eliminate health inequity for all, especially those at risk. Job DescriptionOverview The Clinical Research Registered Nurse (RN) plays a critical role in the successful execution of clinical trials at Mills Clinical Research (MCR). This role integrates clinical nursing practice with research operations to ensure the safe, compliant, and efficient conduct of studies while delivering high-quality, patient-centered care. The RN is responsible for performing protocol-specific procedures, supporting participant recruitment and retention, administering investigational products, and ensuring accurate and timely documentation of clinical and research data. This position works in close collaboration with the Principal Investigator (PI), Sub-Investigators, and Clinical Research Operations leadership to support study implementation and ongoing trial conduct. The Clinical Research RN maintains strict adherence to study protocols, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, HIPAA, FDA regulations, and all applicable state and local requirements. Success in this role requires strong clinical judgment, attention to detail, operational efficiency, and the ability to function within a fast-paced research environment. Essential Functions and Responsibilities (This list may not include all duties assigned.) • Perform protocol-required clinical procedures, including physical assessments, specimen collection, phlebotomy, injections, IV placement and administration, and preparation and administration of investigational products, in accordance with study requirements and physician orders., • Ensure accurate, timely, and complete documentation of all clinical and research activities in source documents, electronic health records, and case report forms (CRFs/eCRFs)., • Support participant recruitment, screening, and enrollment by reviewing medical records, assessing eligibility criteria, and educating potential participants on study requirements., • Obtain and document informed consent in compliance with regulatory and ethical standards prior to initiation of any study-related procedures., • Monitor participant safety by reviewing laboratory results, performing medication reconciliation, identifying, reporting, and promptly escalating adverse events and clinical concerns to the PI and Sub-I., • Dispense investigational products in accordance with protocol, ensuring proper verification, documentation, and participant education., • Collect, process, handle, and ship biological specimens per protocol and laboratory requirements, maintaining chain of custody and specimen integrity., • Collaborate with investigators, director, manager, clinical research coordinators, lab technician, and sponsor representatives to support study conduct, including participation in monitoring visits, audits, and sponsor communications., • Maintain study compliance by adhering to GCP, protocol requirements, SOPs, and regulatory standards; support quality assurance activities and corrective actions as needed., • Provide patient-centered care in a respectful, non-judgmental manner that supports diverse populations and promotes participant engagement and retention., • Educate participants on study procedures, investigational treatments, and follow-up requirements to ensure understanding and protocol adherence., • Maintain a safe and compliant clinical environment by following infection control standards, medication handling procedures, and safety protocols., • Support inventory management of clinical and research supplies, including investigational product accountability as applicable., • Communicate effectively with multidisciplinary teams to ensure continuity of care and operational efficiency across studies., • Participate and prepare for team meetings, protocol trainings, and ongoing education to maintain staff and site competencies and stay current with evolving research and clinical practices., • Provide cross-functional support to research staff, including Director, Manager, Clinical Research Coordinators (CRCs), Medical Assistants (MAs), Investigators, and Providers, as needed to ensure successful study execution., • Perform additional duties as assigned to support clinical and research operations. QUALIFICATIONS • Valid license as a registered nurse (RN) in the state of California required., • Current Basic Life Support certification required., • Experience of working on clinical trials required., • Minimum of three years of experience in direct patient care strongly preferred., • Experience in HIV/AIDS Treatment and Prevention preferred., • Basic knowledge of other infectious diseases and state/federal reporting requirements., • Demonstrate knowledge of effects of psychosocial needs, trauma history, and cognitive/behavioral/motivational functioning on health-related behavior and exhibit ability to intervene appropriately and effectively., • Have the appropriate level of behavioral maturity and patience in handling a variety of patient types and needs., • Must be able to pass a pre-employment drug test, physical, and a background check to include a 7-year criminal, 10-year SSN & employer history reference check., • Must be able to provide proof of COVID-19 vaccination on the first day of work., • Excellent interpersonal skills., • Attention to detail., • Must take yearly flu shot or wear flu mask during flu season for patient-facing positions and test for tuberculosis as required by the Centers for Disease Control and Prevention.

Job DescriptionSenior Automated Litigation Support Lab Manager Employment Type: Full-Time, ExperiencedDepartment: eDiscovery As a CGS Senior ALS Lab Manager, you will leverage industry knowledge, and market research, and have wide-ranging experiences across operating systems and coding languages. You will serve as the lead manager responsible for the delivery of lab data processing services and be responsible for ensuring that incoming productions are made pursuant to the applicable ESI specifications and providing the case attorney with detailed notice of deficiencies. CGS brings motivated, highly skilled, and creative people together to solve the government’s most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities. Skills and attributes for success:- Serves as the lead manager responsible for delivery of lab data processing services.- Primarily ensures timely and accurate completion of tasks. Performs analysis, development and implementation of processing approaches for electronic files and related services pursuant to applicable ESI specifications.- Consults with attorneys and support staff on best practices for conforming to ESI specifications and, as required, participates in teleconferences with co-counsel, client agencies, and opposing counsel upon attorney request.- Responsible for ensuring that incoming productions are made pursuant to the applicable ESI specifications and when deficiencies are found, provides case attorney with detailed notice of deficiencies.- Responsible for keeping the client informed on activities in the Lab, e.g. deadlines, technical challenges, and availability of resources to complete work. - Responsible for webhosting support for unsupported cases managed by the lab.- Manages a team of eDiscovery professionals situated in a client-site eDiscovery laboratory, including: scheduling, requirements assessments, assigning work and ensuring deadlines are met, creating progress reports, and Quality Control (QC) of deliverables.- Advises client attorneys, paralegals, and case managers on all phases of the Electronic Discovery Reference Model (EDRM); especially: Data Collection, Processing, Hosting, Review, Analytics, and Production. Qualifications:- Extensive Relativity experience required.- Relativity certifications including Relativity Certified Administrator (RCA) and/or Relativity Analytics Specialist strongly preferred.- At least eight years of experience performing eDiscovery roles including but not limited to electronic files processing (EFP), image and data file conversion, data culling using review tools, quality assurance, database loads and retrieval, and data analysis and review.- At least five years of experience at the management/supervisory level.- Requires thorough knowledge of the litigation discovery process, and the EDRM workflow.- Working knowledge and certifications of document review software such as iConect, Relativity, Venio or similar tools.- Undergraduate degree required, preferably in computer science or related field. Only the Contracting Officer can approve a waiver of the degree requirement. Ideally, you will also have:- Experience with litigation support tools such as LAW, IPRO, Concordance, MS Office Suite, and LiveNote highly valued. Our Commitment:Contact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client’s specific needs. We are committed to solving the most challenging and dynamic problems. For the past seven years, we’ve been growing our government-contracting portfolio, and along the way, we’ve created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work.Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come. We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Join our team and become part of government innovation!Explore additional job opportunities with CGS on our Job Board: more information about CGS please visit: or contact:Email: #CJ We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer?s Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most r

Voca Healthcare is seeking a travel Radiology Technologist for a travel job in Inglewood, California.Job Description & Requirements.Benefits available on 1st of the month after start:.Are you looking for your next travel assignment or to kick off your traveler career? Voca offers a full benefits pac

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies. Most research studies are conducted remotely at home, though some may be in-person.

Lighthouse Lab Services is the nation's premier medical laboratory consulting, management, and recruiting company.

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies. Most research studies are conducted remotely from home, though some may be in-person. Comfort participating in remote, market r

We are seeking an exceptional Staff Computational Biologist to drive the next generation of software and data products supporting Target Identification and Prioritization across our research organization.

PhD or equivalent research experience in Machine Learning, Natural Language Processing, Statistics, or a related field. You’ll work closely with engineers, product teams, marketing and the broader research community to develop new methods for comparing models, analyzing preference data, and disent